Endo-Kerrison Shaft EKS15554090

GUDID 04250337120261

Endo-Kerrison Shaft

Joimax GmbH

Rigid endoscopic biopsy forceps, reusable

• Primary Device ID: 04250337120261
• NIH Device Record Key: 4e58fa60-e109-4cce-96e4-99ec32819447
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Endo-Kerrison Shaft
• Version Model Number: EKS15554090
• Catalog Number: EKS15554090
• Company DUNS: 344267187
• Company Name: Joimax GmbH
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	04250337120261 [Primary]

FDA Product Code

• LRY: Punch, Surgical

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[04250337120261]

Moist Heat or Steam Sterilization

[04250337120261]

Moist Heat or Steam Sterilization

[04250337120261]

Moist Heat or Steam Sterilization

[04250337120261]

Moist Heat or Steam Sterilization

[04250337120261]

Moist Heat or Steam Sterilization

[04250337120261]

Moist Heat or Steam Sterilization

[04250337120261]

Moist Heat or Steam Sterilization

[04250337120261]

Moist Heat or Steam Sterilization

[04250337120261]

Moist Heat or Steam Sterilization

[04250337120261]

Moist Heat or Steam Sterilization

[04250337120261]

Moist Heat or Steam Sterilization

[04250337120261]

Moist Heat or Steam Sterilization

[04250337120261]

Moist Heat or Steam Sterilization

[04250337120261]

Moist Heat or Steam Sterilization

[04250337120261]

Moist Heat or Steam Sterilization

[04250337120261]

Moist Heat or Steam Sterilization

[04250337120261]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-10-09
• Device Publish Date: 2023-09-29

On-Brand Devices [Endo-Kerrison Shaft]

• 04250337120285: Endo-Kerrison Shaft
• 04250337120278: Endo-Kerrison Shaft
• 04250337120261: Endo-Kerrison Shaft
• 04250337120254: Endo-Kerrison Shaft
• 04250337120247: Endo-Kerrison Shaft